A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583735



Internal ID20956806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12134004..12134709hg38UCSC Ensembl
chr10:12176003..12176708hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38706
hg19706
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233296
Samples
Known GenesSEC61A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583735
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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